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medroxyprogesterone acetate
medroxyprogesterone acetate - 59762-3742-6 - (MEDROXYPROGESTERONE ACETATE)
Drug Information of medroxyprogesterone acetate
| Product NDC: | 59762-3742 |
| Proprietary Name: | medroxyprogesterone acetate |
| Non Proprietary Name: | MEDROXYPROGESTERONE ACETATE |
| Active Ingredient(s): | 10 mg/1 & nbsp; MEDROXYPROGESTERONE ACETATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of medroxyprogesterone acetate
| Product NDC: | 59762-3742 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011839 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19590603 |
Package Information of medroxyprogesterone acetate
| Package NDC: | 59762-3742-6 |
| Package Description: | 50 TABLET in 1 BOTTLE (59762-3742-6) |
NDC Information of medroxyprogesterone acetate
| NDC Code | 59762-3742-6 |
| Proprietary Name | medroxyprogesterone acetate |
| Package Description | 50 TABLET in 1 BOTTLE (59762-3742-6) |
| Product NDC | 59762-3742 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MEDROXYPROGESTERONE ACETATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19590603 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | MEDROXYPROGESTERONE ACETATE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
